rs376790729

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs376790729(C;T)

Make rs376790729(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

45331223

Gene

MUTYH

is a	snp
is	mentioned by
dbSNP	rs376790729
dbSNP (classic)	rs376790729
ClinGen	rs376790729
ebi	rs376790729
HLI	rs376790729
Exac	rs376790729
Gnomad	rs376790729
Varsome	rs376790729
LitVar	rs376790729
Map	rs376790729
PheGenI	rs376790729
Biobank	rs376790729
1000 genomes	rs376790729
hgdp	rs376790729
ensembl	rs376790729
geneview	rs376790729
scholar	rs376790729
google	rs376790729
pharmgkb	rs376790729
gwascentral	rs376790729
openSNP	rs376790729
23andMe	rs376790729
SNPshot	rs376790729
SNPdbe	rs376790729
MSV3d	rs376790729
GWAS Ctlg	rs376790729

Max Magnitude

0

ClinVar
Risk	rs376790729(A;A) rs376790729(T;T)
Alt	rs376790729(A;A) rs376790729(T;T)
Reference	Rs376790729(C;C)
Significance	Pathogenic
Disease	MYH-associated polyposis not provided Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	MUTYH
CLNDBN	MYH-associated polyposis not provided Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000001.10:g.45796895C>A; NC_000001.10:g.45796895C>T
CLNSRC
CLNACC	RCV000234544.2, RCV000487112.1, RCV000165664.2, RCV000200800.3, RCV000480347.1,